Senior Scientist for outsourcing of LCMS Bioanalysis

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Måløv

Are you a qualified and motivated LCMS scientist? Would you like to join our LCMS Bioanalysis department and support the outsourced development projects? Would you like to get involved in developing, validating, and using LC-MS/MS bioanalytical methods for quantitative measurement of drugs, excipients and biomarkers in samples from non-clinical studies and clinical trials? Then this position might be for you, apply today! The position As a Senior Scientist your main focus will be to support the projects with bioanalytical input and data generated at contract research organisations (CRO’s). This includes being responsible scientist (Scientific Monitor) when samples from non-clinical studies and clinical trials are analysed (i.e. no in-house work is expected to be part of this position). Another key task is communication with the projects. Some of your responsibilities will include:
  • Transferring/setting up of new assays at the chosen CRO according to current guidelines.
  • Summarizing assay validations and all sample analysis data in reports for submission fulfilling requirements from the authorities.
  • Representing the Development Bioanalysis Department in cross-functional project teams and collaboration and timely delivery of bioanalytical data and scientific input to stakeholders.
  • Ensuring the right level of bioanalytical science and quality, as well as coordination of activities and timelines.
  • Outsourced dose formulation analysis as well as LCMS biomarker analysis.
    • To ensure a good collaboration with the CRO’s a number of travel days per year must be expected as well as participating in on-line meetings with collaborators from other time zones. Qualifications To be successful in this position you have:
  • A life science academic PhD degree (or similar experience) and minimum 3 years’ experience with development and validation of LC-MS/MS bioanalytical methods.
  • Strong written and oral communication skills in English as well as the capability to work in an interdisciplinary environment.
  • Preferably, familiarity with ICH/EMA/FDA/OECD guidelines and a quality mindset.
  • Flair for use of IT-systems and experience with collaboration with external laboratories is an advantage.
    • About the department The department is responsible for bioanalysis in non-clinical and clinical safety and efficacy evaluations across the entire project portfolio at Novo Nordisk A/S. We are working in a GLP and GCP regulated environment. The department is part of the Global Drug Discovery and located in the Non-clinical and Clinical Assay Sciences in Måløv (Denmark), Novo Nordisk A/S. The LCMS Bioanalysis department currently employs 22 people, 9 technicians and 13 scientists. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Deadline 13 August 2023 Contact For further information, please contact Sune Hove Sporring at +45 30794905. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.


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    Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".

    Arbejdsstedet er beliggende i Måløv.

    Jobbet er oprettet på vores service den 4.7.2023, men kan have været deaktiveret og genaktiveret igen.

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